Canonical Allele Identifier: PA2827968980
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1332383
ClinVar RCV Id: RCV001805429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1748Pro
CA16032957
NM_001354898.2:c.5242A>C